FDADecember 22, 2021device

Destino Twist 14F (also branded as Guidestar 14F)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.

What to do

FDA enforcement status: Completed

Brands named

oscor

UPCs

0088567201112300885672010911

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Destino Twist 14F (also branded as Guidestar 14F) — Recall Details · AllClear